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Prevalence of Permanent Neonatal Diabetes in Slovakia and Successful Replacement of Insulin with Sulfonylurea Therapy in KCNJ11 and ABCC8 Mutation Carriers
CONTEXT: Mutations in the KCNJ11 and ABCC8 genes encoding the pancreatic β-cell K(ATP) channel have recently been shown to be the most common cause of permanent neonatal diabetes mellitus (PNDM). Information regarding the frequency of PNDM has been based mainly on nonpopulation or short-term collect...
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| 出版年: | J Clin Endocrinol Metab |
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| 主要な著者: | , , , , , , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2007
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7611849/ https://ncbi.nlm.nih.gov/pubmed/17213273 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jc.2006-2490 |
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